Labetalol Hydrochloride
NDC 50090-7524, Labetalol Hydrochloride, tablet, film coated, from A-S Medication Solutions.
- Product NDC
- 50090-7524
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209603
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7524 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LABETALOL HYDROCHLORIDE200 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50090-7524-0 | 50090752400 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7524-0) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f9af85d3-a5a7-49d6-aff6-1ca2b2d75450
Use it
Look up 50090-7524 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7524 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-7524. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.